Abdominal obesity and CKD: A potential mediating role of serum metabolites in the UK Biobank population.

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
Hanwen Ye,Hafiz Muhammad Yasir,Jinbo Hu,Wenjin Luo,Yao Qin,Lina Mao,Zhuo Chen,Xiaoru Zhang,Qifu Li,Xiangjun Chen,Zhihong Wang
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Abstract

BACKGROUND It is generally known that although a connection between abdominal obesity and chronic kidney disease (CKD) is well-established, there is a lack of systematic research investigating the specific roles of serum metabolites, including lipid metabolites, amino acid metabolites, carbohydrate metabolites and inflammatory substances in explaining this associations. METHODS We included 118,020 general patients with data of serum metabolites from UK Biobank. We defined abdominal obesity and CKD based on waist circumference and ICD-10 criteria. The serum metabolites were assessed by a high-throughput nuclear magnetic resonance (NMR) based metabolic biomarker profiling platform. We conducted mediation analysis by R software and used the proportion of mediation to quantify the mediation effect. RESULTS This study demonstrated that lipid metabolites played a more important role in mediating the relationship between abdominal obesity and CKD than amino acid metabolites and carbohydrate metabolites. And Glycoprotein Acetyls (GlycA) was the strongest mediator for the correlation between abdominal obesity and CKD, accounting for 26.4 %. And In the mediation analysis stratified by sex, we found that the mediating effects of lipid metabolites were mostly higher in men than in women, while GlycA accounted for the largest proportion of the mediation association in both two groups (31.0 % for women and 19.8 % for men). CONCLUSION Among lipid metabolites, amino acid metabolites, carbohydrate metabolites and inflammatory substances, our study showed that infammation marker GlycA was the novel and key mediator for the correlation between abdominal obesity and CKD.
腹部肥胖与慢性肾脏病:英国生物库人群血清代谢物的潜在中介作用。
背景众所周知,虽然腹部肥胖与慢性肾脏病(CKD)之间的联系已得到证实,但目前还缺乏系统的研究来探讨血清代谢物(包括脂质代谢物、氨基酸代谢物、碳水化合物代谢物和炎症物质)在解释这种关联方面的具体作用。我们根据腰围和 ICD-10 标准定义了腹型肥胖和 CKD。血清代谢物由基于高通量核磁共振(NMR)的代谢生物标记分析平台进行评估。结果本研究表明,脂质代谢物在腹型肥胖与 CKD 关系中的中介作用比氨基酸代谢物和碳水化合物代谢物更重要。糖蛋白乙酰(GlycA)是腹部肥胖与慢性肾脏病之间相关性最强的中介因子,占 26.4%。在按性别分层的中介分析中,我们发现脂质代谢物的中介效应在男性中大多高于女性,而糖蛋白乙酰(GlycA)在两组中介关联中所占比例最大(女性为 31.0%,男性为 19.8%)。结论在脂质代谢物、氨基酸代谢物、碳水化合物代谢物和炎症物质中,我们的研究表明炎症标志物 GlycA 是腹型肥胖与 CKD 相关性的新的关键中介因子。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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